Resection and Reconstruction of Suprahepatic IVC and
Transcription
Resection and Reconstruction of Suprahepatic IVC and
Open Access Case Report DOI: 10.7759/cureus.88 Resection and Reconstruction of Suprahepatic IVC and Right Atrium for Invasive Intrahepatic Cholangiocarcinoma Brian Whang 1, Manoj K. Singh2, Roshan Patel3, Marcelo E. Facciuto4, Arlen G. Fleisher 5 1. Division of Cardiothoracic Surgery, Westchester Medical Center, New York Medical College, Valhalla, New York 2. The Mount Sinai Medical Center 3. Department of Pathology, Westchester Medical Center, New York Medical College 4. Recanati Miller Transplantation Institute, Mount Sinai School of Medicine 5. New York Medical College Corresponding author: Manoj K. Singh, [email protected] Disclosures can be found in Additional Information at the end of the article Abstract Surgical resection of intrahepatic cholangiocarcinoma with major vascular and atrial invasion is described in this case report using cardiopulmonary bypass followed by complex vascular reconstruction. Categories: Cardiac/Thoracic/Vascular Surgery, Pathology, General Surgery Keywords: cholangiocarcinoma, atrium, hepatic tumor, cardiopulmonary bypass, surgery Introduction Cholangiocarcinoma is a primary hepatic tumor that arises from the biliary ductal epithelium. Early symptoms are uncommon unless it occurs at or distal to the hepatic duct bifurcation, so many patients present with large, often unresectable tumors. Here we report the case of an intrahepatic cholangiocarcinoma invading the suprahepatic inferior vena cava (IVC) and right atrium, along with our surgical approach and technique for reconstruction. Case Presentation A 47 year-old woman was incidentally found to have a liver mass during workup for an asymptomatic umbilical hernia. Computed tomography of the abdomen and pelvis demonstrated a non-enhancing 3 cm mass in the left aspect of the caudate lobe of the liver. This mass was adjacent to the inferior vena cava and appeared to invade the left hepatic vein and extend superiorly to the right atrium. Received 01/19/2013 Review began 01/19/2013 Published 01/29/2013 © Copyright 2013 Whang et al. This is an open access article distributed under the terms of the Creative Commons Attribution License CC-BY 3.0., which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. The patient was referred for surgical resection. The operation was performed with a team of hepatobiliary and cardiothoracic surgeons. First, abdominal exploration was done through a bilateral subcostal incision with midline extension. Upon palpation, the tumor invaded the suprahepatic IVC, the surrounding diaphragm, and extended into the right atrium. A left hepatectomy, including caudate lobe resection, starting with parenchymal transection was performed, leaving only the left and middle hepatic veins attached to the IVC. Next, a median sternotomy was performed, the cava were snared, the liver vascular inflow was controlled with a vascular clamp. The patient was placed on cardiopulmonary bypass with the inferior vena cava cannula inserted distal to the hepatic veins, the superior cava cannulated through the right atrial appendage, and the arterial cannula in the ascending aorta. The cava was then opened 1 cm caudal to the entrance of the left hepatic vein. The tumor was palpated superiorly past the atriocaval junction. The inferior portion of the right atrium was resected 2 mm below the How to cite this article Whang B, Singh M K, Patel R, et al. (2013-01-29 21:56:49 UTC) Resection and Reconstruction of Suprahepatic IVC and Right Atrium for Invasive Intrahepatic Cholangiocarcinoma. Cureus 5(1): e88. DOI 10.7759/cureus.88 coronary sinus. The entire en bloc specimen was then removed from the operative field, which included the left lobe and caudate lobe of the liver, IVC, diaphragm, and right atrium (Figure 1). FIGURE 1: Pathological specimen showing extent of tumor spread. The atriocaval junction was then reconstructed using 34 mm Hemashield tube graft (Boston Scientific, Natick, MA) (Figure 2). 2013 Whang et al. Cureus 5(1): e88. DOI 10.7759/cureus.88 2 of 5 FIGURE 2: Reconstructed atriocaval junction with 34mm Hemashield graft. The right atrium was resected 2mm below the coronary sinus. The inferior part of the graft was tailored to the preserved back wall and distal inferior vena cava just above the cannula. When this was completed, the patient was easily weaned from bypass and decannulated. The diaphragm was then reconstructed using Gore-Tex mesh (Gore, Tempe, AZ). The patient’s postoperative course was uneventful. Ultrasound of the liver demonstrated graft patency, and the patient was placed on low molecular-weight heparin to prevent thrombosis of the graft. Final pathology revealed infiltrating, poorly differentiated cholangiocarcinoma invading the left hepatic vein and extended through liver capsule and diaphragm into the wall of the right atrium. Discussion Surgical resection is the gold standard for cholangiocarcinoma. While chemotherapy, external beam radiation, and a combination of the two have been studied, there has not been compelling evidence to support the use of these modalities outside of a trial setting [1]. Some specialized centers have taken an aggressive surgical approach to tumors that invade adjacent vascular structures, and extended hepatic resections with caval reconstruction have been successfully performed [1,2]. Five-year survival for intrahepatic cholangiocarcinoma ranges from 8% to 47%, depending upon the ability to achieve negative (R0) margins [1]. Lang et al. have achieved a median survival of 46 months with a calculated one- and three-year survival rate of 94% and 82%, respectively, for R0 resection [2]. However, the median survival drops to five months for R1 resection (microscopic tumor at margins), and the calculated one-year survival is 22%. Stage greater than I, multifocality, lymph node involvement, and vascular invasion are poor prognostic factors [2]. 2013 Whang et al. Cureus 5(1): e88. DOI 10.7759/cureus.88 3 of 5 Intracardiac extension of hepatic tumors presents an even greater challenge to resectability. There are some advanced cases that have presented with Budd-Chiari syndrome [3,4]. While there are scant reports in the literature describing the successful resection of hepatocellular carcinoma with extension to the heart, there is no such documentation for cholangiocarcinoma [4-7]. Removal of the tumor without disturbing its integrity precludes traditional methods of vascular control. Facciuto et al. and Azoulay et al. describe several techniques for the resection of tumors at the hepatocaval confluence, including total vascular exclusion with transdiaphragmatic intrapericardial control of the cava, veno-venous bypass, and in situ hypothermic perfusion of the liver [8,9]. However, the presence of tumor within a cardiac chamber requires the application of cardiopulmonary bypass (CPB) for resection. The success of this technique and its positive impact on survival have been demonstrated in the extirpation of hepatocellular and renal cell carcinoma [7,10-12]. Invasion of the heart and great vessels by thoracic malignancies have also been successfully treated with aggressive resection on cardiopulmonary bypass. Park et al. have shown that the use of CPB itself did not lead to major morbidity, and that curative resection can be safely achieved [13]. Conclusions Hepatic tumors with extensive local invasion involving major vascular and cardiac chambers can be safely resected. The literature supports an aggressive surgical approach and the use of CPB if the tumor can be completely resected and requires complex vascular reconstruction. Our patient presented with an intrahepatic cholangiocarcinoma, a tumor whose mainstay of treatment is surgical resection. A team approach between specialized hepatobiliary and cardiothoracic surgeons enabled complete extirpation of the tumor. Additional Information Disclosures Conflicts of interest: The authors have declared that no conflicts of interest exist. References 1. 2. 3. 4. 5. 6. 7. 8. 9. Khan SA, Thomas HC, Davidson BR, Taylor-Robinson SD: Cholangiocarcinoma. Lancet. 2005, 366:1303-14. 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